LRRC59 — 49 ClinVar variants

All ClinVar germline LRRC59 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 45 flagged for review →

1 Benign · 2 Likely benign · 46 Uncertain significance

Full LRRC59 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 45

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

Predictors lean, ClinVar uncertain 30

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All LRRC59 variants

Benign 1

Likely benign 2

Uncertain significance 46